System and method for neuromodulation

ABSTRACT

A method of treating a patient having a blood pressure comprises delivering neuromodulation therapy to sustain or increase the blood pressure. The neuromodulation therapy includes placing a sympathetic therapy electrode in a posterior portion of a blood vessel and stimulating at least one extravascular cardiac sympathetic nerve fiber using said electrode.

PRIORITY

This application is a continuation of U.S. application Ser. No.14/516,734, filed Oct. 17, 2014 (Attorney Docket IAC-1261), which is acontinuation U.S. application Ser. No. 13/547,031, U.S. Pat. No.9,067,071, filed Jul. 11, 2012 (Attorney Docket IAC-1260), which claimsthe benefit of U.S. Provisional Application No. 61/506,164, filed Jul.11, 2011 (Attorney Docket IAC-1200), U.S. Provisional Application No.61/551,418, filed Oct. 25, 2011 (Attorney Docket IAC-1210), U.S.Provisional Application No. 61/584,812, filed Jan. 9, 2012 (AttorneyDocket IAC-1220), U.S. Provisional Application No. 61/601,501, filedFeb. 21, 2012 (Attorney Docket IAC-1230), U.S. Provisional ApplicationNo. 61/613,433, filed Mar. 20, 2012 (Attorney Docket IAC-1240), and U.S.Provisional Application No. 61/639,982, filed Apr. 29, 2012 (AttorneyDocket IAC-1250). Each of the foregoing applications is incorporatedherein by reference.

TECHNICAL FIELD OF THE INVENTION

The present application generally relates to systems and methods forneuromodulation using stimulation elements disposed within thevasculature.

BACKGROUND

Acute heart failure syndromes (AHFS) are serious conditions resulting inmillions of hospitalizations each year. Well documented in theliterature are causal links between declining renal function ormyocardial injury during AHFS hospitalization and poor prognosis. Heartfailure resulting from myocardial ischemic insult or tachycardiaprecipitates complex alterations in autonomic tone, neurohormonalactivation, and the inflammatory metabolic state. These changes inautonomic tone are typically manifested by increased heart rate and areduction in heart rate variability. In the setting of an acuteexacerbation of heart failure, the dramatically elevated heart rate isfrequently accompanied by hypotension. The critical role of treating theautonomic nervous system dysfunction observed in HF has long beenrecognized (with inotropic agents and beta-blockers). Recently, specificneuromodulation of the parasympathetic cardiac nerve inputs has shownsignificant therapeutic benefit. Cleland JG, Bristow MR, Erdmann E,Remme W J, Swedberg K, Waagstein F. Beta-blocking agents in heartfailure. Should they be used and how? Eur Heart J 1996; 17:1629-39; DeFerrari G M, Crijns H J, Borggrefe M, et al. Chronic vagus nervestimulation: a new and promising therapeutic approach for chronic heartfailure. Eur Heart J 2011; 32:847-55.

However, in the case of AHFS associated with congestive symptoms andreduced blood pressure (BP), the negative inotropic effects of loneparasympathetic intervention or beta-blockade can severely limit theirutility. In the face of hypotension, sympathetic tone must be maintainedin order to assure adequate left ventricular (LV) contractility. Anand IS, Fisher L D, Chiang Y T, et al. Changes in brain natriuretic peptideand norepinephrine over time and mortality and morbidity in theValsartan Heart Failure Trial (Val-HeFT). Circulation 2003; 107:1278-83.Animal studies have demonstrated positive inotropic effects (increasedLV pressure and cardiac output without change in systemic vascularresistance) when selectively stimulating certain cardiac efferentsympathetic nerves. Zarse M, Plisiene J, Mischke K, et al. Selectiveincrease of cardiac neuronal sympathetic tone: a catheter-based accessto modulate left ventricular contractility. J Am Coll Cardiol 2005;46:1354-9; Meyer C, Rana O R, Saygili E, et al. Augmentation of leftventricular contractility by cardiac sympathetic neural stimulation.Circulation 2010; 121:1286-94.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 graphically represents stimulation effects achievable using thedisclosed system and method.

FIG. 2A is a top, cross-section view of the superior vena cavaillustrating a target electrode region for delivery of therapy toparasypathetic and sympathetic targets.

FIG. 2B is similar to FIG. 2A and schematically shows electrodespositioned to deliver therapy to the parasympathetic and sympathetictargets.

FIG. 3 schematically illustrates a therapy device disposed with thesuperior vena cava to position electrodes between the superior venacava's bifurcation and the atrium of the heart.

FIG. 4 schematically illustrates an embodiment of a control system for aneuromodulation system.

FIG. 5 is a graphical representation illustrating control of normalcardiovascular function by the autonomic nervous system's cardiovascularcontrol system.

FIG. 6 is a graphical representation illustrating an adjustedcardiovascular control system achieved through the addition of thedisclosed neuromodulation system to the autonomic nervous system'scardiovascular control system.

DETAILED DESCRIPTION

The present application discloses methods and systems for treatingautonomic imbalance in a patient by energizing a first therapeuticelement disposed in a superior vena cava of the patient to delivertherapy to a parasympathetic nerve fiber such as a vagus nerve, andenergizing a second therapeutic element disposed within the superiorvena cava to deliver therapy to a sympathetic cardiac nerve fiber. Aneuromodulation system includes a parasympathetic therapy elementadapted for positioning within a blood vessel, a sympathetic therapyelement adapted for positioning with the blood vessel; and a stimulator.The stimulator is configured to energize the parasympathetic therapyelement to deliver parasympathetic therapy to a parasympathetic nervefiber disposed external to the blood vessel and energize the sympathetictherapy element within the blood vessel to deliver sympathetic therapyto a sympathetic nerve fiber disposed external to the blood vessel. Indisclosed embodiments, delivery of the parasympathetic and sympathetictherapy can be used to decrease the patient's heart rate and whileelevating or maintaining the blood pressure of the patient.

Studies conducted by the inventors have elucidated distinct and precisesites in the superior vena cava (SVC) where neurostimulation selectivelyresults in modulation of both cardiac parasympathetic and sympatheticnerves. These anatomic locations were demonstrated using minimallyinvasive, vascular procedures. These studies demonstrated thatindependent cardiac parasympathetic and sympathetic stimulation isachievable from fully intravascular locations within the SVC. Theresults of these studies consistently demonstrated that parasympatheticneuromodulation through vagus nerve stimulation to decrease heart rate(HR) with attendant effect on blood pressure (BP) is simple,straightforward and repeatable. The studies also revealed thatsympathetic neuromodulation for the purpose of increasing BP withattendant effect on HR could also be accomplished in a straightforwardmanner.

The present inventors have achieved rapid, acute parasympathetic andsympathetic modulation of cardiac hemodynamics in humans usingintravascular stimulation of the vagus nerve and cardiac sympatheticbranches from within the SVC. In those studies, stimulation parametersof 5-15 mA, 20 Hz, and 0.5 ms pulse width were shown to be effective.

Although other investigators have separately stimulated parasympatheticor sympathetic nerves to cardiac effect using surgically-basedapproaches, no previous approaches have demonstrated simultaneous andselective modulation of both autonomic inputs from intravascularlocations. This unprecedented advantage of instantaneous and completeflexibility in management of HR and BP, together with an easy-to-use,minimally invasive approach will provide substantial therapeuticbenefit.

The disclosed system can provide a broad spectrum of clinically relevantcontrol through its ability to modulate both HR and BP. In patients thatrequire a decrease in HR and BP, such as those with diastolic heartfailure and preserved ejection fraction that present with elevated HRand BP, pure parasympathetic stimulation is provided (lower left handbox of FIG. 1). Similarly, for those patients requiring pure sympatheticstimulation, such as for elevation of heart rate and blood pressure(upper right hand box) the system provides that capability. But in manycases of acute decompensation, particularly in those patientsapproaching or in cardiogenic shock or with cardiorenal syndrome, pureparasympathetic or pure sympathetic stimulation could have potentialdetrimental effects. These patients often present with both hypotensionand tachycardia. Pure parasympathetic stimulation could worsen thissituation by simultaneously decreasing heart rate while potentiallyreducing blood pressure resulting in inadequate systemic perfusion. Onthe other hand, pure sympathetic stimulation, while supporting the bloodpressure, could further drive the existent tachycardia to extremelevels. Ideally, under the condition of hypotension and tachycardia dueto these forms of heart failure, one would want to provide support ofthe blood pressure to provide for adequate systemic perfusion whilesimultaneously reducing tachycardia and even lowering the heart ratefurther to allow adequate cycle length to optimize the stroke volume,preserving or improving cardiac output (upper left hand box), atreatment achievable using the disclosed system.

Ultimately, a combination of autonomic modulation based on hemodynamicfeedback of both HR and BP would provide optimal therapy.

While discussed in connection with acute heart failure syndrome, thedisclosed system and methods may be used to provide acute autonomicneuromodulation in patients suffering from other conditions, including,but not limited to acute myocardial infarction, pulmonary embolism,hemorrhage, autonomic dysfunction, systemic inflammatory response,syndrome (SIRS), sepsis, as well as post-surgery autonomic dysfunction.Moreover, principles disclosed herein may further be implemented usingan implantable system, including one in which the electrodes arechronically disposed or anchored in the SVC at positions determined todeliver the disclosed parasympathetic and/or sympathetic stimulus. Animplantable system may have an implantable stimulator, such as oneimplanted at an intravascular or extravascular (e.g. subcutaneous) site,or a stimulator that is positioned outside the body for wirelesslyactivating the electrodes. Applications for a chronic system includetreatment of patients suffering from chronic heart failure, or autonomicdysfunction associated with other conditions including those listedabove.

Accordingly, the present inventors have conceived of a system that issuitable for each type of neuromodulation represented in FIG. 1,including delivery of independent and simultaneous stimulation ofparasympathetic and sympathetic cardiac nerves to achieve a simultaneousreduction in HR and increase in BP that results in an increase incardiac output. Referring to FIG. 3, the neuromodulation systemcomprises a therapy device 10 having one or more intravasculartherapeutic elements 12 a, 12 b. The therapy device 10 positions thetherapeutic elements within the SVC, where they are selectivelyenergized to modulate nerve fibers located outside the vasculature. Thetherapeutic elements are arranged such that some of the therapeuticelements (referred to herein as the parasympathetic therapeutic elements12 a) direct energy to parasympathetic cardiac nerve fibers from withinthe SVC, while different ones of the therapeutic elements (referred toas the sympathetic therapeutic elements 12 b) direct energy tosympathetic cardiac nerve fibers, also from within the SVC. See FIG. 2B.Because percutaneous advancement of a catheter to the SVC is a simpleand straightforward procedure, the ability to position bothparasympathetic and sympathetic therapeutic elements within the SVC ishighly advantageous.

In preferred embodiments, the therapeutic elements 12 a, b areelectrodes 14, although it is contemplated that other forms oftherapeutic elements (including, but not limited to, ultrasound,thermal, or optical elements) may instead be used. The therapeuticelements are positioned on a flexible therapy device such as a catheteror other flexible elongate carrier 16, allowing advancement of thetherapeutic elements from a percutaneous access site to the SVC. Thetherapy device includes an anchoring structure 18 expandable within thevasculature for biasing the electrodes in contact with the interiorsurface of the blood vessel so as to optimize conduction ofneuromodulation energy from the electrodes to the target nerve fibers.

The therapy device or catheter and its corresponding electrodes andanchoring structure may take a variety of forms. Reference is made tocommonly-owned Application Nos. PCT/US12/35712 (“Neuromodulation Systemsand Methods for Treating Acute Heart Failure Syndromes”; Atty Docket:IAC-1010), U.S. Ser. No. 13/547,035, filed Jul. 11, 2012 (“CatheterSystem for Acute Neuromodulation; Atty Docket: IAC-1201), each of whichis fully incorporated herein by reference. These applications describeexemplary electrode and catheter systems for use in acuteneuromodulation which may be used or adapted for use with the disclosedneuromodulation system. Electrodes disclosed in U.S. application Ser.No. 13/281,399 entitled Intravascular Electrodes and Anchoring Devicesfor Transvenous Stimulation, may also be adapted for use with thedisclosed system.

A preferred therapy device for use in the disclosed method utilizes anintegrated design, from which stimulus may be directed from a singleintravascular therapy device to two or more nerve targets. A device ofthis type may include a single flexible support 16 or cathetersupporting multiple electrodes 18 or electrode arrays which may beindependently activated to stimulate a different nerve target. In thistype of embodiment, the multiple electrodes (i.e. those used forparasympathetic stimulation and those used for sympathetic stimulation)may be supported by a common support or electrode carrying member 18that biases the electrodes into contact with the vessel wall. Forexample, the electrode carrying member 18 might be formed of two or morelongitudinal splines carried by the support 16 in an arrangement of thetype disclosed in the prior applications incorporated herein(schematically shown in FIG. 3). With this design, the parasympatheticstimulation electrodes may be a bipolar arrangement of electrodeslongitudinally arranged on a first spline, and the sympatheticstimulation electrodes may be a bipolar arrangement of electrodeslongitudinally arranged on a second spline of the catheter. As anotherexample, the parasympathetic stimulation electrodes and the sympatheticstimulation electrodes may be positioned on a common expandable sleeveformed of mesh, laser cut tubing, or other structures used forendoluminal electrode supports or stents.

The electrode carrying member 18 may include multiple splines or regionshaving electrode arrays. This arrangement allows a mapping procedure tobe conducted upon placement of the catheter within the SVC, such thatthe splines/regions whose electrodes produce the most optimalparasympathetic and sympathetic response may be determined and used fortreatment. In other words, mapping may be used to determine which ofmultiple electrodes or electrode arrays will be the parasympatheticstimulation electrodes or arrays, and which will be the sympatheticstimulation electrodes or arrays.

In other embodiments, the electrode carrying member supports a firstelectrode, electrode array, or electrode pair for parasympathetic use,and a second electrode, electrode array, or pair for sympathetic use,together with means for independently or simultaneously adjusting thepositions of the first and second arrays during mapping. Other electrodearrangements may be used, including separate catheters (e.g. telescopingor parallel catheters) for sympathetic and parasympathetic stimulation,with each catheter having longitudinally spaced electrodes. In these andthe prior examples, independent bipolar electrodes, bipolar electrodessharing a common pole, or unipolar electrodes may be used—withindifferent electrodes in the unipolar embodiments positioned elsewhereon the catheter or in/on the patient.

An external stimulator 20 energizes the electrodes using stimulationparameters selected to capture the target nerve fibers and to achievethe desired neuromodulation.

Suitable stimulation parameters are 5-15 mA, 20 Hz, and 0.5 ms pulsewidth, although other stimulation parameters may alternatively be used.Feedback to the stimulator is provided by one or more diagnosticsensors. The catheter and stimulator may operate as a closed-loopsystem, allowing simulation parameters to be automatically determinedand/or dynamically controlled in response to information sensed by thesensors and/or derived from sensor feedback. Suitable sensed or derivedhemodynamic parameters may include central venous pressure (CVP),pulmonary capillary wedge pressure (PCWP), cardiac index, derivations ofvascular resistance, heart rate, blood pressure (arterial). Otherparameters may include CO/CI, and cardiac filling pressures. For someparameters such as CVP, feedback may be generated using sensors mountedon the electrode-carrying member or extending through the lumen of itscatheter.

Electrode Position

The therapy device 10 positions the electrodes 14 or other therapyelements such that simultaneous sympathetic and parasympatheticstimulation may be carried out using parasympathetic stimulationelectrodes disposed in the postero-lateral segment of the mid to cranialportion of the Superior Vena Cava, and sympathetic stimulationelectrodes disposed in the postero-medial segment of the mid to cranialportion of the Superior Vena Cava.

In preferred methods, the electrode positions in the SVC from which theparasympathetic (vagus) PS and cardiac sympathetic nerve branches S maybe stimulated reside in a zone Z within an approximately 120-270 degreecircumferential band centered on the posterior wall of the vessel. Inother words, referring to FIG. 2A, if mid-anterior MA is considered tobe at 0 degrees (6 o'clock in FIG. 2A below), proceeding clockwise,electrodes may be positioned on the vessel wall within a region thatextends along the vessel wall from 45 to 315 degrees. In otherembodiments, electrodes may be positioned on the vessel wall within aregion that extends along the vessel wall from 120-240 degrees asidentified in FIG. 2A. The electrode(s) 12 a used for parasympatheticstimulation is/are preferably positioned on the postero-lateral side,and the sympathetic electrode(s) 12 b is/are positioned on thepostero-medial side as shown in FIG. 2B. In some embodiments, theelectrodes are disposed in the same horizontal plane as shown in FIG.2B, although in other embodiments the electrodes may be longitudinallyoffset from one another. Stimulation electrodes are preferablypositioned away from portions of the SVC wall that are proximate toextravascular nerves whose stimulation would produce undesirableeffects. One such collateral stimulation zone C is disposed on theanterior-lateral wall as shown in FIG. 2A.

As shown in FIG. 3, the electrodes 14 are positioned in the portion ofthe SVC disposed between the SVC's bifurcation and the atrium of theheart.

Control System

FIG. 4 schematically illustrates one embodiment of a neuromodulationsystem, including a control system 100 suitable for carrying out thetherapy disclosed herein. The neuromodulation system includes atherapeutic catheter 10 having therapeutic elements 12 a, 12 b, 14, suchas electrode arrays, and optionally, patient and system diagnosticelements; sensors 15 (e.g. pressure sensors, flow sensors, otherhemodynamic sensors, other patient condition sensors, and systemcondition sensors such as position sensors, system connection sensors orother system error condition monitoring sensors). The neuromodulationsystem also includes an external stimulator, (labeled “NeuroModulator”in the drawing). The external stimulator has a clinician user interfaceand functions to provide therapeutic stimulation outputs to thetherapeutic catheter; therapeutic outputs that are dynamicallycontrolled in a closed-loop manner in response to information from oneor more of the diagnostic elements. The diagnostic elements includesensors for patient hemodynamic feedback such as heart rate (HR), bloodpressure (BP), and other suitable sensed or derived hemodynamicparameters (which may include central venous pressure (CVP), pulmonarycapillary wedge pressure (PCWP), cardiac index, derivations of vascularresistance, cardiac output, and cardiac filling pressures); sensorsand/or analyzers to determine other patient conditions such as cardiacarrhythmia, cardiac capture, respiration, or patient movement; and othersensors and analyzers to monitor system conditions for error,malfunction or unsafe state (referred to as “safety monitoring”) thatshould be indicated to the clinician and/or result in termination ofstimulation. Together, these system components form a control systemthat is capable of safely balancing both parasympathetic and sympathetictone to achieve the clinically desired HR and BP conditions, just as inthe native autonomic nervous system.

The unique advantage of this autonomic system modulation is theutilization of simultaneous and selective modulation of bothparasympathetic and sympathetic inputs directly to the heart fromdistinct sites completely in the vasculature, but ideally within acommon blood vessel. The complete flexibility in the management of HRand BP in combination with a minimally invasive, percutaneous approachto access the direct autonomic inputs to the heart provides asubstantial advantage in the treatment of clinical conditions such asacute heart failure syndrome (AHFS). Normal cardiovascular function iscontrolled by the autonomic nervous system's cardiovascular controlsystem, a negative feedback system, in which increased BP and cardiacoutput increases afferent activity which inhibits sympathetic activityand activates parasympathetic activity, while decreased BP and cardiacoutput decreases afferent activity, resulting in the opposite effect, asshown in FIG. 5. In FIGS. 5 and 6, the following references are used: B(brain), P (parasympathetic activity), S (sympathetic activity), H(heart), FH (failed heart), A (afferents, sensory inputs), R (receptors,throughout the system), V (vasculature), I (adjusted inputs to heart),stim (stimulation).

In the case of decompensated heart failure, however, since the heart isdamaged, the effective transfer function of the heart is perturbed, ascardiac output is depressed despite higher HR which leads todecompensation of the entire cardiovascular system, and the negativefeedback cardiovascular control system can no longer functionappropriately. The failing heart is being driven with sympatheticexcitation due to the lowered BP and cardiac output sensed by theafferent nerves, which leads to further diminished cardiacoutput—effectively, the system now operates at a point of decompensationdue to the changed transfer function of the failing heart. Theneuromodulation system has the ability to alter the inputs directly atthe heart in an immediate, minimally invasive manner so that the failingheart can be controlled in a manner more suitable for its currentcondition. This immediately changes the operating point of thecardiovascular control system to a clinically appropriate point, wheretreatment of the acute decompensation, such as with inotropic agents ordiuresis, can be safely conducted with the autonomic system operating ata more suitable state. The addition of the neuromodulation system allowsa new, adjusted cardiovascular control system as depicted in FIG. 6.Furthermore, the closed-loop control options afforded by simultaneousand selective parasympathetic and sympathetic stimulation allows theneuromodulation system to adapt as the patient's condition improves andthe operating point of the system moves away from the decompensatedstate. The neuromodulation system can then minimize its contribution tothe heart's direct neural inputs as the system begins functioning morenormally.

Utilizing this control system, the neuromodulation system provides twoprimary functions: a continuous safety-monitored, closed-loop control tomodulate heart rate (HR) and blood pressure (BP) with user-specifiedboundaries for the ultimate purpose of controlling patient hemodynamics;and an automatic parasympathetic and sympathetic response mappingfunction for the ultimate purpose of selecting the ideal electrodes tostimulate target nerves.

The control system, shown in FIG. 4, contains a Parasympathetic Control210 function, a Sympathetic Control function 212, a Safety Monitoringfunction 228, a Parasympathetic Stimulation Output function 214, aSympathetic Stimulation Output function 216, an Electrode Switchingfunction 218, and a number of other system feedback elements, consistingof sensors, analyzers and detectors of various system and patientconditions. The control system elements or functions can be implementedindividually as or any combination of electronic circuitry, computersubsystems, computer software, mechanical subsystems, ultrasoundsubsystems, magnetic subsystems, electromagnetic subsystems, opticalsubsystems, and a variety of sensors or detectors including, but notlimited to, electromechanical sensors, electrochemical sensors, thermalsensors, and infrared sensors. The control system elements or functionscommunicate with each other by direct physical means (electrically wiredconnection, mechanical interaction) or other indirect means (such aswireless RF, visible light, infrared, sound, ultrasound).

The Parasympathetic and Sympathetic Output functions generate thetherapeutic stimuli that can be, but are not limited to, electricalpulses. These two output functions can generate independent therapeuticlevels (for example, electrical currents, voltages, and pulse widths),timing (frequencies, triggers or gates to other timing such as ECGevents, the latter of which might be used, for example, to initiatestimulation during the atrial refractory period), and polarity (asapplicable). The two output functions allow independent parasympatheticand sympathetic therapeutic outputs to be generated and delivered to thetherapy catheter's therapeutic elements, described as electrodes.

The Electrode Switching function 218 provides the means to connect theParasympathetic and Sympathetic Output functions to the desiredelectrodes on the therapy catheter's electrode array so as to capturethe target cardiac nerves fibers (i.e., the parasympathetic nerve fibersto the Parasympathetic Output function and the sympathetic nerve fibersto the Sympathetic Output function). The selection of which connectionor connections to make is determined during the response mappingprocedure, described later in this application.

The Parasympathetic and Sympathetic Control functions implement thesystem's overall function based on user inputs 232 (target HR and BPboundaries, or immediate output disable 234) and feedback from patientsensed or hemodynamic parameters, as well as system diagnosticconditions for safety monitoring. The Parasympathetic and SympatheticControl functions directly govern the therapeutic output fromParasympathetic and Sympathetic Output functions, respectively, bycontrolling the therapeutic levels, timing, polarity, as well as theability to disable the outputs. The Control functions are responsiblefor, at a minimum, the two primary functions of the neuromodulationsystem: the closed-loop modulation of HR and BP, as well as the responsemapping function. In one example, the Parasympathetic and SympatheticControl functions implement closed loop modulation utilizing theuser-targeted HR and BP boundaries, as well as the feedback from actualHR and BP. Also, in other examples, additional sensed and/or derivedhemodynamic parameters (such as flow rates, cardiac output, etc.described above) can also be determined by the system and used inaddition to, or in place of, HR and BP. The transfer functionimplemented by the Parasympathetic and Sympathetic Control functions canbe linear or non-linear in nature. For example, although the HR and BPfeedback response may be linear within a given range of modulation,non-linear response may occur at other points. Also, an input from theSafety Monitoring function may require a non-linear response to protectpatient safety.

The Safety Monitoring function 228 receives inputs from the variouspatient and system diagnostic functions for the purpose of monitoringthe safety of the system. The Safety Monitoring function can output tothe Parasympathetic and Sympathetic Control functions to alter thetherapeutic outputs to the patient and/or initiate a clinician alarm orindicator 230. The purpose of these outputs is to ensure that theneuromodulation system's therapeutic outputs are providing stimulationto the patient only when the system believes the state of the patientand system monitored conditions are in a known defined state, describedin this applications as “safe”. For example, a patient condition thatmay be monitored by the Safety Monitoring function is the presence ofinadvertent atrial capture by the therapeutic neurostimulation. Thisstate would be undesirable from a clinical perspective because thetherapeutic stimulation intended for nerve capture is capturingmyocardium, and the Safety Monitoring function would, in this example,communicate to the immediately disable the therapeutic output from thesystem. Another example of a patient condition would be the cardiac ECGto control the timing of the therapeutic outputs with respect to thecardiac cycle such as synchronizing stimulation to the heart. Anotherexample of a patient condition would be any suitable sensed or derivedhemodynamic parameter (such as flow rates, cardiac output, etc.described above) that is clinically unsafe and should result in eitheran alarm or disabling of therapeutic output. There are also a variety ofsystem conditions that shall be monitored by the Safety Monitoringfunction, including, but not limited to, a connection failure to thetherapy catheter, monitoring central venous pressure to determine if thetherapy catheter position is anatomically correct, and an externalstimulator malfunction (such as electrical circuit failure, computermalfunction, software malfunction, mechanical malfunction, etc.) Anysystem condition that can be sensed or derived from the system's sensorsis monitored by the Safety Monitoring function.

The neuromodulation system also contains patient and system feedbackelements that sense, measure or derive various patient and systemconditions and provide this information to both the Parasympathetic andSympathetic Control functions and the Safety Monitoring function. Thesefeedback elements include sensors on the therapy catheter 10 such aspressure sensors, flow sensors, thermal sensors, P02 sensors, mechanicalinteracting component, magnetic components, as well as the therapeuticelectrodes and additional sensing electrodes. In addition, clinicalsensors used directly on the patient such as arterial pressuretransducers, ECG electrodes, and other hemodynamic monitors can beutilized and connected to the external stimulator. For example, feedbackof arterial blood pressure and heart rate are key to the performance ofthe neuromodulation system. An Arterial Blood Pressure Sensor function220 that would be connected to a standard arterial line pressuretransducer can be utilized to determine BP and HR for the controlsystem. Therapy catheter electrodes or surface ECG electrodes can beconnected to an ECG Analyzer function 222 that would derive ECGparameters such as HR, P and R-wave timing, refractory timing, andpresence of cardiac arrhythmias, such as tachycardia or fibrillation,can be utilized as inputs to the system or for safety monitoring. OtherHemodynamic Sensors 242 can be used to sense or derive hemodynamicparameters (such as flow rates, cardiac output, temperature, P02 etc.described above) can be used both for closed-loop control, as well assafety monitoring. A Central Venous Pressure Sensor 240 is disclosed toprovide feedback both on the therapy catheter's position, as well ashemodynamic feedback that can be utilized as part of the closed-loopcontrol system. A Cardiac Capture Detector function 224 can be utilizedto check if the neurostimulation therapy is unintentionally capturingthe atrium due to incorrect catheter position and may induce arrhythmia.A Catheter Connection Detector 236 that is comprised of, for example, amagnetic or proximity sensor can be used to assure the therapy catheterand external stimulator connection integrity, and a Catheter PositionSensor 238 can be utilized to assure that the catheter anatomicplacement is stable during system usage. Other Safety Monitoring Sensors226 may also be provided throughout the system to detect malfunctions(such as electrical circuit failure, computer malfunction, softwaremalfunction, mechanical malfunction, etc.) or other unsafe.

Method

An exemplary method for using an integrated device to achievehemodynamic control will next be described. This method is particularlyuseful for decreasing heart rate and increasing or maintaining bloodpressure in the treatment of acute heart failure syndrome.

First, the integrated catheter is percutaneously delivered to thesuperior vena cava (e.g. using access through the femoral vein,subclavian, or internal jugular vein). The electrode carrying member ispositioned in the SVC between the bifurcation and the top of the atrium,and the electrodes are brought into contact with the surrounding wallsof the SVC, preferably such that the electrodes contact the posteriorwall of the SVC. Electrode contact is preferably achieved by expandingthe electrode carrying member within the SVC, as described in the priorapplications incorporated herein.

Mapping is performed to identify the optimal electrode location. Thismapping may be either manually controlled by the clinician orautomatically controlled utilizing the external stimulator and electrodecarrying members on the catheter. Where the electrode carrying membersupports multiple arrays of electrodes, each array is independentlyenergized and the response measured until the optimal array for theparasympathetic stimulation is identified and until the optimal arrayfor the sympathetic stimulation is identified. Where the electrodecarrying member supports a single array for parasympathetic use and asingle array for sympathetic use, the arrays are energized and theresponse measured. The arrays may be repositioned and the test repeateduntil the optimal positions for the parasympathetic and sympatheticarrays are identified. In either case, mapping includes aparasympathetic mapping step in which electrodes on the postero-lateralsegment of the SVC are energized, and a sympathetic mapping step inwhich electrodes on the postero-medial segment of the SVC are energized.

During the parasympathetic mapping step, heart rate is monitored priorto and then during energization of the electrodes disposed on the SVC'spostero-lateral segment. If the heart rate during stimulation does notdecrease by at least a threshold amount, for example at least 5%, asecond parasympathetic site is selected by repositioning theparasympathetic array or by energizing another array located on thepostero-lateral wall of the SVC. The process is repeated until astimulation site is determined that will decrease the heart rate by atleast the threshold amount (which in this example is 5%).

During the sympathetic mapping step, heart rate and/or blood pressure ismonitored prior to and during energization of the electrodes on thepostero-medial segment. If the heart rate and/or blood pressure duringstimulation does not increase by at least a threshold amount, forexample 5%, a second sympathetic site is selected by repositioning thesympathetic array or by energizing another array located on thepostero-medial wall of the SVC. The process is repeated until astimulation site is determined that will increase the blood pressure byat least the threshold amount (which in this example is 5%). Note thateven where the desired therapy is to lower HR and sustain or elevate BP,identification of a target sympathetic stimulation site might stillinclude monitoring for an increase in heart rate by at least a thresholdamount during energization of the electrodes being positioned forsympathetic stimulation. This is because an elevation in heart rateduring sympathetic mapping confirms that sympathetic cardiac nerves arebeing captured by the sympathetic side stimulus.

The parasympathetic and sympathetic mapping steps may be performedsimultaneously or separately. Where each of these steps is performedseparately, during the sympathetic mapping step, the electrodes on thepostero-lateral segment of the SVC are preferably not energized, andlikewise during the parasympathetic mapping step electrodes on thepostero-medial segment of the SVC are preferably not energized. Analternative sympathetic mapping step, which is performed after theparasympathetic stimulation site has been identified, involvesconducting sympathetic mapping while simultaneously deliveringparasympathetic stimulation from the identified parasympatheticstimulation site. In this example, a sympathetic electrode site might bechosen that allows the patient's blood pressure to be maintained despitethe decreased HR associated with the parasympathetic stimulation.

Mapping may further include adjusting the stimulation parameters (e.g.amplitude, frequency and pulse width) and observing the response whilethe electrodes remain at a given electrode location so as to identifythe optimal stimulation parameters.

In some embodiments, mapping is automatic, such that the user sets thetarget heart rate and blood pressure values and the system selects thestimulation parameters and/or electrode position based on the measuredresponse to stimulus during mapping.

Once the parasympathetic and sympathetic electrodes are determined to bein suitable positions to achieve the desired stimulation of the targetnerves, treatment is initiated. The parasympathetic and sympatheticelectrodes may be energized simultaneously, or the parasympathetic andsympathetic stimulation may be alternated. Where the parasympathetic andsympathetic therapeutic energy is delivered at separate times, it mayoccur at separate times asynchronously to each other, or separately, butsynchronized to each other The stimulation parameters for theparasympathetic and sympathetic electrodes may be the same or they maybe different.

For treatment of acute heart failure syndrome, the neuromodulation maybe used to lower the patient's heart rate and raise or maintain thepatient's blood pressure. Target heart rates fall in a range of 30-180beats per minute (bpm), preferably 45-140 bpm, and most preferably60-100 bpm. Target systolic blood pressures, with the patient in asupine position, fall in a range of 70-180 mmHg, preferably 80-150 mmHg,and most preferably 90-120 mmHg.

By providing simultaneous stimulation of parasympathetic nerves andsympathetic cardiac nerve fibers, the system may operate such thatstimulation of one system (e.g. the parasympathetic or sympatheticnervous system) augments or mollifies the other system in a manner thatproduces the desired physiologic outcome. One particular benefit of sucha system is its ability to respond to detection of a diminishedphysiological response resulting from adaptation of the autonomicnervous system (ANS) to a particular set of stimulation parameters. Forexample, in use the system is set up to deliver parasympathetic andsympathetic stimulations to produce a desired range of heart rate andblood pressure. It is recognized that there are various combinations ofthe sympathetic and parasympathetic stimulus that will achieve thetarget heart rate and blood pressure ranges. As the body adapts to theparticular combination of stimuli being delivered by the system, thesystem will sense a diminution of the physiological response, and willthus begin to apply a different combination of parasympathetic andsympathetic stimulation that will produce the target HR and BP ranges.Alternatively, the system may be programmed to periodically shift fromone combination of parasympathetic and sympathetic stimulationparameters to another combination, so as to avoid adaptation by the ANS.Where the catheter includes multiple electrode arrays, the system mightfurther be programmed to periodically alter which of the arrays is usedto deliver stimulus, as yet another safeguard against adaptation.

Referring again to FIG. 1 above, the system may alternatively beoperated to decrease both heart rate and blood pressure by solely orprimarily energizing the parasympathetic electrodes. One suitableapplication for this mode is the treatment of tachycardia. In anothermode of operation, the pulse generator is used to solely or primarilyenergize the sympathetic electrodes in order to increase blood pressure,such as for treatment of hypotension.

While in this application use of the sympathetic stimulation has focusedon use of the sympathetic stimulation to maintain or elevate bloodpressure, in other alternative methods sympathetic electrodes in the SVCmay instead be used to stimulate sympathetic cardiac nerves that areprimarily associated with chronotropic or dromotropic effects.

Experimental Results

In an experimental arrangement, separate catheters were positioned inthe SVC at the positions described in the preceding paragraphs. Stimuluswas delivered at 20 Hz, Pulse Width=0.5 ms, and Amplitude of 10 mA foreach catheter. Stimulus was performed on each catheter simultaneouslyfrom electrodes (4 mm separation) in a vertical plane. The distancebetween the two catheters was about 1-2 cm and at an estimated 45degrees circular.

As discussed above, similar electrode arrangements can be achievedthrough a variety of different catheter designs, including but notlimited to electrode placement on the splines of a catheter of the typedescribed in the incorporated applications, allowing the parasympatheticstimulation electrodes and the sympathetic stimulation electrodes toreside on a single catheter and yet to be placed at distinct, separate,areas for the optimal stimulation of parasympathetic and the sympatheticnerves. The figures discussed above illustrate the positioning of such acatheter with the SVC.

The animal study was designed to evaluate the hemodynamic effects ofsimultaneously modulating both parasympathetic and sympathetic cardiacefferent nerves via intravascular stimulation at distinct sites in thesuperior vena cava (SVC).

In an initial study using two canines, a 12Fr sheath was placed via theSeldinger technique in the right femoral vein and a second 12Fr sheathwas positioned in left femoral vein. Separate sheaths were employed inthese experiments in order to maximize stability and minimizeinteraction between catheters. A 7Fr and 6Fr sheath were introduced intothe right and left femoral arteries, respectively. Arterial accessallowed left ventriculogram acquisition and continuous BP monitoring.Two guide catheters containing 8Fr standard quadripolar stimulationcatheters were introduced from the femoral veins and employed toidentify the optimal region for parasympathetic and sympatheticstimulation in the SVC, which was easily achieved. Once the stimulationsite was located, the catheters were maintained in the same position forthe duration of the study.

In both canine subjects, dual channel, simultaneous neurostimulation wasapplied to each catheter. Stimulation durations of approximately 1-2minutes were repeated to assure reproducibility of hemodynamic effect.Pharmacologic intervention intended to block parasympathetic effect wasalso administered during stimulation (Atropine, 0.5 mg IV).

Based on the findings from the first canine experiment, the secondcanine experiment was modified to include increased time periodcontinuous stimulation, measurement of ejection fraction, and the use ofbeta blockade (propranolol) to confirm sympathetic stimulation effect.Therefore, the second canine was subjected to continuous dual channelstimulation for 1 hour with continuous monitoring. Also, in the secondcanine, the Atropine was followed 5 minutes later by beta-blockerpropranolol (3 mg IV for two doses). Finally, in the second canine, apigtail catheter was placed in the left ventricle and ventriculogramsfor the purpose of measuring ejection fraction obtained at baseline andduring dual stimulation.

The first canine experiment (Test #1) resulted in the finding that thenovel, fully intravascular, simultaneous, dual channel stimulation ofboth parasympathetic and sympathetic cardiac efferent nerves can beachieved, and results in remarkable HR decrease together with BPelevation. Also, administration of Atropine confirmed that the resultingHR decrease was solely due to the parasympathetic stimulation.

The second canine experiment (Test #2) easily confirmed the samefindings as seen in Test #1, in addition to successful 1 hour continuousstimulation, an increase in ejection fraction, and the use of betablockade confirmed sympathetic stimulation effect.

Three additional canine experiments were then conducted to confirm thefindings as seen in the first two experiments. The same procedure wasutilized, and in addition, direct cardiac output measurements were takenin Tests #4 and Test #5 utilizing an invasive flow measurement catheter.

The five consecutive canine experiments provided consistent confirmationthat independent control of HR and BP was achieved. In particular, lowerHR simultaneous with higher BP was consistently demonstrated. Theeffects were demonstrated acutely and over the course of an hour.Ejection fraction and cardiac output were improved. Targeted drug usedemonstrated the target neuromodulation effects.

The animal study was designed to evaluate the hemodynamic effects ofsimultaneously modulating both parasympathetic and sympathetic cardiacefferent nerves via intravascular stimulation at distinct sites in thesuperior vena cava (SVC). The experimental results are summarized asfollows:

-   -   In all five (5) canines, parasympathetic stimulation-only        resulted in a significant decrease in HR with attendant effects        on BP and sympathetic stimulation-only demonstrated an increase        in HR and BP as seen in earlier studies    -   In all five (5) canines, simultaneous parasympathetic and        sympathetic dual stimulation resulted in a decrease of HR and an        increase or maintenance in BP    -   After cessation of stimulation, all five canines returned to        baseline hemodynamic parameters within 1-3 minutes    -   In two of two canines in which the measurement was taken, the        ejection fraction improved measurably during dual stimulation    -   In two of two canines in which the measurement was taken, the        cardiac output was preserved or improved measurably during dual        stimulation despite the reduction in HR    -   In four of four canines in which the measurement was taken, the        HR and BP response was maintained for 1 hour of stimulation and        when stimulation was discontinued, the HR returned to baseline        within 10 seconds with baseline BP returning within 1-3 minutes    -   In all five (5) canines, Atropine administration eliminated        stimulation-induced HR reduction confirming selective        parasympathetic modulation    -   Also, in four of four canines in which the measurement was        taken, propranolol administration mitigated stimulation-induced        BP response confirming selective sympathetic modulation

The results of the five canine studies are set forth in Table 1 below:

TABLE 1 Stimulation Data Para- sympathetic Sympathetic Dual Dual StimAtropine Propanolol Test # Stim Stim Stim (after 1 hour) Effect Effect 1Δ HR

 87 bpm

 2 bpm

 87 bpm ✓

 52%

 1%

 53% Δ BP

 7 mmHg

 24 mmHg

 25 mmHg

 4%

 15%

 16% 2^(i) Δ HR

 63 bpm

 3 bpm

 35 bpm

 46 bpm ✓ ✓

 47%

 3%

 26%

 35% Δ BP

 6 mmHg

 25 mmHg

 35 mmHg

 29 mmHg

 3%

 31%

 36%

 27% 3 Δ HR

 94 bpm

 39 bpm

 58 bpm

 79 bpm ✓ ✓

 61%

 26%

 37%

 48% Δ BP

 35 mmHg

 18 mmHg

 31 mmHg

 14 mmHg

 16%

 9%

 14%

 7% 4^(ii) Δ HR

 53 bpm

 11 bpm

 54 bpm

 44 bpm ✓ ✓

 35%

 7%

 38%

 30% Δ BP

 3 mmHg

 16 mmHg

 14 mmHg

 50 mmHg

 1%

 7%

 7%

 23% 5^(iii) Δ HR

 48 bpm

 60 bpm

 44 bpm

 25 bpm ✓ ✓

 38%

 55%

 34%

 19% Δ BP

 23 mmHg

 13 mmHg

 30 mmHg

 29 mmHg

 11%

 7%

 15%

 14% ^(i)Ejection Fraction: No stim = 67%, with stim = 72% ^(ii)EjectionFraction: No stim = 41%, with stim = 55% Cardiac Output: No stim = 4.6L/min, with stim = 5.1 L/min ^(iii)Cardiac Output: No stim = 5.9 L/min,with stim = 6.8 L/min

We claim:
 1. A method of treating a patient having a blood pressure,comprising: delivering neuromodulation therapy to sustain or increasethe blood pressure, said neuromodulating therapy including placing asympathetic therapy electrode in a posterior portion of a blood vesseland stimulating at least one extravascular cardiac sympathetic nervefiber using said electrode.
 2. The method of claim 1, further includingintroducing a therapy device into the vasculature, the therapy devicehaving the electrode thereon, and advancing the therapy device withinthe vasculature to position the electrode in the posterior portion ofthe blood vessel.
 3. The method of claim 1 the placing step positionsthe electrode in venous vasculature superior to the heart.
 4. The methodof claim 3, wherein the placing step positions the electrode in thesuperior vena cava.
 5. The method of claim 4 wherein the placing stepincludes positioning the electrode in a segment of the superior venacava extending between a right atrium and a junction of brachiocephalicveins.
 6. The method of claim 1, further including energizing the firstand second electrodes using a stimulator disposed external to thepatient.
 7. The method of claim 1, further including monitoring bloodpressure and heart rate of the patient, and modifying stimulus from theelectrode in response to detected changes in heart rate and/or bloodpressure.